autosomal recessive nonsyndromic deafness 121

Term ID

DOID:0070675

Synonyms

• DFNB121

Definition

An autosomal recessive nonsyndromic deafness characterized by congenital or prelingual moderate sensorineural hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in the GPR156 gene on chromosome 3q13. https://pmc.ncbi.nlm.nih.gov/articles/PMC10562426/

References

• MIM:620551

Ontology

Human Disease   ( DOID:0070675 )